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GlyTouCan
Glycan Structure Repository
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Glycoconjugate Repository
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Glycomics MS raw data Repository
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Glycomics MS Repository for glycan annotations from GlycoWorkbench
LM-GlycoRepo
Repository for lectin-assisted multimodality data
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Genes / Proteins / Lipids Glycans / Glycoconjugates Glycomes Pathways / Interactions / Diseases / Organisms
Alliance of Genome Resources
Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.
| Source | Last Updated |
|---|---|
| Alliance of Genome Resources | October 9, 2024 |
| Disease ID | Disease Name | Alliance of Genome Resources ID | Species | Gene ID | Gene Symbol ▼ | FlyGlycoDB | Evidence Code Names | References |
|---|---|---|---|---|---|---|---|---|
| DOID:0110731 | neuronal ceroid lipofuscinosis 3 | HGNC:2024 | Homo sapiens (human) | 1185 | CLCN6 |
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| DOID:3393 | coronary artery disease | HGNC:2024 | Homo sapiens (human) | 1185 | CLCN6 |
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| DOID:0080353 | X-linked recessive hypophosphatemic rickets | HGNC:2023 | Homo sapiens (human) | 1184 | CLCN5 |
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| DOID:0111815 | low molecular weight proteinuria with hypercalciuric nephrocalcinosis | HGNC:2023 | Homo sapiens (human) | 1184 | CLCN5 |
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| DOID:0050699 | Dent disease | HGNC:2023 | Homo sapiens (human) | 1184 | CLCN5 |
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| DOID:447 | renal tubular transport disease | HGNC:2023 | Homo sapiens (human) | 1184 | CLCN5 |
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| DOID:0111798 | X-linked nephrolithiasis type I | HGNC:2023 | Homo sapiens (human) | 1184 | CLCN5 |
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| DOID:13533 | osteopetrosis | HGNC:2023 | Homo sapiens (human) | 1184 | CLCN5 |
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| DOID:0050699 | Dent disease | HGNC:2021 | Homo sapiens (human) | 1182 | CLCN3 |
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| DOID:13533 | osteopetrosis | HGNC:2021 | Homo sapiens (human) | 1182 | CLCN3 |
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| DOID:0111815 | low molecular weight proteinuria with hypercalciuric nephrocalcinosis | HGNC:2021 | Homo sapiens (human) | 1182 | CLCN3 |
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| DOID:0110731 | neuronal ceroid lipofuscinosis 3 | HGNC:2021 | Homo sapiens (human) | 1182 | CLCN3 |
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| DOID:423 | myopathy | HGNC:2020 | Homo sapiens (human) | 1181 | CLCN2 |
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| DOID:0111312 | idiopathic generalized epilepsy 11 | HGNC:2020 | Homo sapiens (human) | 1181 | CLCN2 |
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| DOID:10579 | leukodystrophy | HGNC:2020 | Homo sapiens (human) | 1181 | CLCN2 |
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| DOID:1485 | cystic fibrosis | HGNC:2020 | Homo sapiens (human) | 1181 | CLCN2 |
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| DOID:446 | primary hyperaldosteronism | HGNC:2020 | Homo sapiens (human) | 1181 | CLCN2 |
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| DOID:0080330 | cold-induced sweating syndrome 2 | HGNC:17412 | Homo sapiens (human) | 23529 | CLCF1 |
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| DOID:2945 | severe acute respiratory syndrome | HGNC:17412 | Homo sapiens (human) | 23529 | CLCF1 |
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| DOID:0110355 | retinitis pigmentosa 32 | HGNC:29675 | Homo sapiens (human) | 23155 | CLCC1 |
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| DOID:1485 | cystic fibrosis | HGNC:2015 | Homo sapiens (human) | 1179 | CLCA1 |
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| DOID:3083 | chronic obstructive pulmonary disease | HGNC:2015 | Homo sapiens (human) | 1179 | CLCA1 |
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| DOID:2841 | asthma | HGNC:2015 | Homo sapiens (human) | 1179 | CLCA1 |
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| DOID:1824 | status epilepticus | HGNC:1995 | Homo sapiens (human) | 1159 | CKMT1B |
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| DOID:1824 | status epilepticus | HGNC:31736 | Homo sapiens (human) | 548596 | CKMT1A |
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